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无水共聚合:极性非水溶剂中的脂质自组装。

Getting together without water: Lipid self-assembly in polar non-aqueous solvents.

机构信息

School of Science, RMIT University, Melbourne, VIC 3000, Australia.

School of Science, RMIT University, Melbourne, VIC 3000, Australia.

出版信息

Eur J Pharm Biopharm. 2024 Nov;204:114472. doi: 10.1016/j.ejpb.2024.114472. Epub 2024 Aug 24.

Abstract

Self-assembled structures have numerous applications including drug delivery, solubilization, and food science. However, to date investigations into self-assembled structures have been largely limited to water, with some additives. This limits the types of assemblies that can form, as well as the accessible temperature range. Non-aqueous, polar solvents such as ionic liquids and deep eutectic solvents offer alternative self-assembly media that can overcome many of these challenges. These novel solvents can be designed to support specific types of assemblies or to remain stable under more extreme conditions. This review highlights recent advances in the field of self-assembly in polar non-aqueous solvents. Here we quantify the contribution of certain solvent properties such as nanostructure and solvent cohesion to lipid self-assembly. While this field is still relatively new, preliminary design rules are emerging, such as increasing hydrophobic regions leading to decreasing solvent cohesion, with a consequent reduction in lipid phase diversity. Ultimately, this review demonstrates the capacity for solvent control of lipid assemblies while also drawing attention to areas that need further work. With more systematic studies, solvents could be explicitly designed to achieve specific lipid assemblies for use in target applications, such as cargo delivery to particular cell types (e.g. cancerous), or triggered release under desired conditions (e.g. pH for release on wound infection).

摘要

自组装结构在许多领域都有应用,包括药物输送、增溶和食品科学。然而,迄今为止,自组装结构的研究主要局限于水和一些添加剂。这限制了可以形成的组装类型,以及可访问的温度范围。非水、极性溶剂,如离子液体和深共晶溶剂,提供了替代的自组装介质,可以克服许多这些挑战。这些新型溶剂可以设计为支持特定类型的组装,或在更极端的条件下保持稳定。本综述重点介绍了极性非水溶剂中自组装领域的最新进展。在这里,我们量化了某些溶剂性质(如纳米结构和溶剂内聚能)对脂质自组装的贡献。虽然这个领域还相对较新,但初步的设计规则正在出现,例如增加疏水区会导致溶剂内聚能降低,从而导致脂质相多样性降低。最终,本综述展示了溶剂对脂质组装的控制能力,同时也引起了对需要进一步研究的领域的关注。通过更系统的研究,可以明确设计溶剂以实现特定的脂质组装,用于目标应用,例如将货物递送到特定类型的细胞(例如癌细胞),或在所需条件下触发释放(例如 pH 值用于伤口感染时的释放)。

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